Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore 169857, Singapore.
Institute of Molecular and Cell Biology (IMCB), Agency for Science, Technology and Research (A*STAR), Singapore 138673, Singapore.
Viruses. 2024 Oct 21;16(10):1646. doi: 10.3390/v16101646.
Inflammasome is linked to many inflammatory diseases, including COVID-19 and autoimmune liver diseases. While severe COVID-19 was reported to exacerbate liver failure, we report a fatal acute-on-chronic liver failure (ACLF) in a stable primary biliary cholangitis-autoimmune hepatitis overlap syndrome patient triggered by a mild COVID-19 infection. Postmortem liver biopsy showed sparse SARS-CoV-2-infected macrophages with extensive ASC (apoptosis-associated speck-like protein containing a CARD) speck-positive hepatocytes, correlating with elevated circulating ASC specks and inflammatory cytokines, and depleted blood monocyte subsets, indicating widespread liver inflammasome activation. This first report of a fatal inflammatory cascade in an autoimmune liver disease triggered by a mild remote viral infection hopes to elucidate a less-described pathophysiology of ACLF that could prompt consideration of new diagnostic and therapeutic options.
炎症小体与许多炎症性疾病有关,包括 COVID-19 和自身免疫性肝病。虽然有报道称严重的 COVID-19 会加重肝功能衰竭,但我们报告了一例稳定的原发性胆汁性胆管炎-自身免疫性肝炎重叠综合征患者,因轻度 COVID-19 感染引发致命性的慢加急性肝衰竭(ACLF)。尸检肝活检显示稀疏的 SARS-CoV-2 感染巨噬细胞,伴有广泛的 ASC(含 CARD 的凋亡相关斑点样蛋白)斑点阳性肝细胞,与循环 ASC 斑点和炎症细胞因子升高以及血液单核细胞亚群耗竭相关,提示广泛的肝脏炎症小体激活。这是首例由轻度远程病毒感染引发的自身免疫性肝病中致命炎症级联反应的报告,希望阐明 ACLF 的一种描述较少的病理生理学,这可能促使考虑新的诊断和治疗选择。